Biomet, Inc. recalls
6 recalls on record · FDA
Every recall we have on record for Biomet, Inc., compiled from federal safety data. Check the hazard, the remedy, and how serious each one is, and always confirm on the official notice.
Vanguard Knee System AS Tibial Bearing / DCM ArCom, 12 MM X 75 MM; Model Number 189082.…
Possible damage to the Vanguard Knee System AS Tibial Bearing caused during the manufacturing process.
Compress Device Short Anchor Plug, 26 MM-For Correction of revision of unsuccessful…
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Compress Device Short Anchor Plug, 24 MM-For Correction of revision of unsuccessful…
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Compress Device Short Anchor Plug, 14 MM-For Correction of revision of unsuccessful…
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Compress Device Short Anchor Plug, 28 MM-For Correction of revision of unsuccessful…
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number…
The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner.